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Infect. Immun., 04 1996, 1227-1232, Vol 64, No. 4
MJ Karim, SC Basak and AJ Trees
The oocyst wall of Eimeria spp. consists of a 10-nm-thick outer lipid layer
and a 90-mm-thick inner layer of glycoprotein which has been described
previously to be composed of a single major protein. Sodium dodecyl
sulfate-polyacrylamide gel electrophoresis under reducing conditions and
(125)I labelling of a oocyst wall fragments and of delipidated intact
oocysts revealed a molecule of approximately 12 kDa as the major protein
component of the oocyst wall of Eimeria tenella. An immunoglobulin M
monoclonal antibody (c11B9F3) was produced against this 12-kDa oocyst wall
protein sliced from a preparative SDS- polyacrylamide gel. Its reactivity
by immunofluorescence against oocyst wall fragments and sporozoites or by
immunoperoxidase assays of infected tissue sections was stage restricted to
gametocytes and oocysts but pan-specific against all face of the oocyst
wall. In chicks passively immunized with C11B9F3, oocyst output was
significantly (P<0.01) reduced by 42 to 54% after homologous E. tenella
infection and by 35% after heterologous Eimeria maxima infection compared
with that of control groups. The results demonstrate the presence of a
highly conserved, low-molecular-weight antigen on the oocyst wall and the
gametocytes of Eimeria spp. which is a candidate for inclusion in a pan-
specific, transmission-blocking vaccine against avian coccidiosis.
Copyright © 1996, American Society for Microbiology
Characterization and immunoprotective properties of a monoclonal antibody against the major oocyst wall protein of Eimeria tenella
Veterinary Parasitology, Liverpool School of Tropical Medicine, United Kingdom.
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